Hemminki K - Search Results

1

Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia.

Vijayakrishnan J, Studd J, Broderick P, Kinnersley B, Holroyd A, Law PJ, Kumar R, Allan JM, Harrison CJ, Moorman AV, Vora A, Roman E, Rachakonda S, Kinsey SE, Sheridan E, Thompson PD, Irving JA, Koehler R, Hoffmann P, Nöthen MM, Heilmann-Heimbach S, Jöckel KH, Easton DF, Pharaoh PDP, Dunning AM, Peto J, Canzian F, Swerdlow A, Eeles RA, Kote-Jarai Z, Muir K, Pashayan N; PRACTICAL Consortium; Greaves M, Zimmerman M, Bartram CR, Schrappe M, Stanulla M, Hemminki K, Houlston RS. Vijayakrishnan J, et al. Among authors: hemminki k. Nat Commun. 2018 Apr 9;9(1):1340. doi: 10.1038/s41467-018-03178-z. Nat Commun. 2018. PMID: 29632299 Free PMC article.

2

Separation of 7-methyl- and 7-(2-hydroxyethyl)-guanine adducts in human DNA samples using a combination of TLC and HPLC.

Kumar R, Hemminki K. Kumar R, et al. Among authors: hemminki k. Carcinogenesis. 1996 Mar;17(3):485-92. doi: 10.1093/carcin/17.3.485. Carcinogenesis. 1996. PMID: 8631134

3

Correspondence re: Zheng et al, Haplotype of two variants in p16 (CDKN2/MTS-1/INK4a) exon 3 and risk of squamous cell carcinoma of the head and neck: a case-control study. 11: 640-645, 2002.

Kumar R, Hemminki K. Kumar R, et al. Among authors: hemminki k. Cancer Epidemiol Biomarkers Prev. 2003 Jan;12(1):71; author reply 72. Cancer Epidemiol Biomarkers Prev. 2003. PMID: 12540508 No abstract available.

4

Simultaneous detection of the exon 10 polymorphism and a novel intronic single base insertion polymorphism in the XPD gene using single strand conformation polymorphism.

Kumar R, Angelini S, Hemminki K. Kumar R, et al. Among authors: hemminki k. Mutagenesis. 2003 Mar;18(2):207-9. doi: 10.1093/mutage/18.2.207. Mutagenesis. 2003. PMID: 12621078

5

Activating BRAF and N-Ras mutations in sporadic primary melanomas: an inverse association with allelic loss on chromosome 9.

Kumar R, Angelini S, Hemminki K. Kumar R, et al. Among authors: hemminki k. Oncogene. 2003 Dec 18;22(58):9217-24. doi: 10.1038/sj.onc.1206909. Oncogene. 2003. PMID: 14681681

6

BRAF mutations are common somatic events in melanocytic nevi.

Kumar R, Angelini S, Snellman E, Hemminki K. Kumar R, et al. Among authors: hemminki k. J Invest Dermatol. 2004 Feb;122(2):342-8. doi: 10.1046/j.0022-202X.2004.22225.x. J Invest Dermatol. 2004. PMID: 15009715 Free article.

7

Mutations in the BRAF and N-ras genes in childhood acute lymphoblastic leukaemia.

Gustafsson B, Angelini S, Sander B, Christensson B, Hemminki K, Kumar R. Gustafsson B, et al. Among authors: hemminki k. Leukemia. 2005 Feb;19(2):310-2. doi: 10.1038/sj.leu.2403589. Leukemia. 2005. PMID: 15538400 No abstract available.

8

The rare ERBB2 variant Ile654Val is associated with an increased familial breast cancer risk.

Frank B, Hemminki K, Wirtenberger M, Bermejo JL, Bugert P, Klaes R, Schmutzler RK, Wappenschmidt B, Bartram CR, Burwinkel B. Frank B, et al. Among authors: hemminki k. Carcinogenesis. 2005 Mar;26(3):643-7. doi: 10.1093/carcin/bgh342. Epub 2004 Nov 18. Carcinogenesis. 2005. PMID: 15550452 Free article.

9

c-MYC Asn11Ser is associated with increased risk for familial breast cancer.

Wirtenberger M, Hemminki K, Försti A, Klaes R, Schmutzler RK, Grzybowska E, Bermejo JL, Wappenschmidt B, Bugert P, Butkiewicz D, Pamula J, Pekala W, Zientek H, Bartram CR, Burwinkel B. Wirtenberger M, et al. Among authors: hemminki k. Int J Cancer. 2005 Nov 20;117(4):638-42. doi: 10.1002/ijc.21225. Int J Cancer. 2005. PMID: 15929079 Free article.

10

Association of death receptor 4 haplotype 626C-683C with an increased breast cancer risk.

Frank B, Hemminki K, Shanmugam KS, Meindl A, Klaes R, Schmutzler RK, Wappenschmidt B, Untch M, Bugert P, Bartram CR, Burwinkel B. Frank B, et al. Among authors: hemminki k. Carcinogenesis. 2005 Nov;26(11):1975-7. doi: 10.1093/carcin/bgi164. Epub 2005 Jun 23. Carcinogenesis. 2005. PMID: 15975957

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